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* Centro de Estudos de Ciência Animal do Institutode Ciências e Tecnologias Agrárias e Agro-Alimentares,
Faculdade de Ciências, and
Instituto de Ciências Biomédicas de Abel Salazar, Universidade do Porto, Campus Agrário de Vairão, Rua Padre Armando Quintas,4485-661 Vairão VC, Portugal
Institute of Grassland and Environmental Research, Plas Gogerddan, Aberystwyth, Ceredigion SY23 3EB, UK
Corresponding author: A. R. J. Cabrita; e-mail: rita.cabrita{at}mail.icav.up.pt.
The effects of N supplementation strategies on milk fatty acid profiles of dairy cows and their use as a noninvasive technique to diagnose rumen function, and to guide protein feeding decisions on-farm were evaluated in three experiments. Each experiment was designed according to three 3 x 3 Latin squares with 9 Holstein cows receiving total mixed rations based on corn silage. Experiment 1 was designed to study effects of diets with different ratios of effective rumen-degradable protein (ERDP; g) to fermentable metabolizable energy (FME; j) providing, respectively, a large deficiency, a slight deficiency, and a slight excess in relation to the target level of 11 g of ERDP/MJ FME for lactating cows. Experiment 2 evaluated effects of different proportions of quickly and slowly rumen-degradable protein achieved by replacing soybean meal with urea in the concentrates (0, 0.5, and 1% urea for U0, U5, and U10, respectively). Experiment 3 investigated effects of synchronizing the availability of FME and ERDP in rumen by offering the protein-rich concentrate once or twice per day before the meal (corn silage, ryegrass hay, and energy-rich concentrate), or included in the total mixed ration. Milk fatty acid profiles were significantly affected by dietary N and carbohydrate supply. Principal component factor analysis provided a reasonable description of the data, clearly discriminating between fatty acids that are synthesized by different metabolic pathways. Several sources/pathways were distinguished: de novo synthesis in the mammary gland (short- and medium-chain fatty acids),
9-desaturase activity (monoenoic fatty acids), direct absorption from the blood stream (long-chain fatty acids), and de novo synthesis by the rumen microbial populations (odd-chain fatty acids). Discriminant canonical analysis showed that milk odd-chain fatty acids had a higher ability to discriminate between diets than even-chain fatty acids. The anteiso C15:0 increased in line with increasing sugar supply, and C17:0 appears to be a marker of protein deficiency. Additionally, iso C17:0 and anteiso C17:0 were associated with the NDF and CP contents of diets. The results suggests that milk odd-chain fatty acids have the potential to be used as a noninvasive technique to assess rumen function in terms of microbial populations, substrates and interactions.
Key Words: bovine milk fatty acid profile nitrogen supplementation rumen function
Abbreviation key: D1 = protein-rich concentrate fed once a day before the a.m. meal, D2 = protein-rich concentrate fed twice a day before both meals, DU = protein-rich concentrate given with the basal diet, ERDP = effective rumen-degradable protein, FME = fermentable metabolizable energy, QDP = quickly rumen-degradable protein, RH = diet with a slight excess of ERDP in relation to FME, RL = diet with a large deficiency of ERDP in relation to FME, RM = diet with a slight deficiency of ERDP in relation to FME, SDP = slowly rumen-degradable protein, U0 = concentrate with 0% urea, U5 = concentrate with 0.5% urea, U10 = concentrate with 1% urea
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